Evidence map›Paper›PMID 17166848›Full record

ArticleThe Journal of biological chemistry2007

Tumor-specific and proliferation-specific gene expression typifies murine transgenic B cell lymphomagenesis.

Marc E Lenburg, Anupama Sinha, Douglas V Faller, Gerald V Denis

Open access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of biological chemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  5. Clinical trials for BET inhibitors run ahead of the science.Drug discovery today. Technologies · 2016
    Review
  6. Review
  7. Article
  8. BRD4 inhibitor inhibits colorectal cancer growth and metastasis.International journal of molecular sciences · 2015
    Article
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  13. High-dose infusional gemcitabine combined with busulfan and melphalan with autologous stem-cell transplantation in patients with refractory lymphoid malignancies.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2012
    Article
  14. Article
  15. Review
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  19. Article
  20. Double bromodomain-containing gene Brd2 is essential for embryonic development in mouse.Developmental dynamics : an official publication of the American Association of Anatomists · 2009
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Marc E LenburgDepartment of Genetics and Genomics, and Boston University School of Medicine, Boston, Massachusetts 02118.
Anupama SinhaCancer Research Center, Boston University School of Medicine, Boston, Massachusetts 02118.
Douglas V FallerCancer Research Center, Boston University School of Medicine, Boston, Massachusetts 02118.
Gerald V DenisCancer Research Center, Boston University School of Medicine, Boston, Massachusetts 02118. Electronic address: gdenis@bu.edu.
Boston University · USCancer Research Center · US

Funding

NOVEL, INDUCIBLE NUCLEAR KINASE LINKED TO LEUKEMIAR29CA075107 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DENIS, GERALD V · 1997 to 2001
$242k
Proteomic biomarkers for lymphomaR03CA128006 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DENIS, GERALD V · 2007 to 2008
$163k
Biomarkers for lymphoma in a new transgenic mouse modelR03CA102889 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DENIS, GERALD V · 2004 to 2005
$162k
NCI NIH HHS CA102889NCI NIH HHS CA75107NCI NIH HHS R03 CA102889NCI NIH HHS R03 CA128006NCI NIH HHS R29 CA075107
6 · The paper itself

Abstract

The dual bromodomain protein Brd2 is closely related to the basal transcription factor TAF(II)250, which is essential for cyclin A transactivation and mammalian cell cycle progression. In transgenic mice, constitutive lymphoid expression of Brd2 causes a malignancy most similar to human diffuse large B cell lymphoma. We compare the genome-wide transcriptional expression profiles of these lymphomas with those of proliferating and resting normal B cells. Transgenic tumors reproducibly show differential expression of a large number of genes important for cell cycle control and lymphocyte biology; expression patterns are either tumor-specific or proliferation-specific. Several of their human orthologs have been implicated in human lymphomagenesis. Others correlate with human disease survival time. BRD2 is underexpressed in some subtypes of human lymphoma and these subtypes display a number of similarities to the BRD2-mediated murine tumors. We illustrate with a high degree of detail that cancer is more than rampant cellular proliferation, but involves the additional transcriptional mobilization of many genes, some of them poorly characterized, which show a tumor-specific pattern of gene expression.

Indexed as

Gene Expression Regulation, LeukemicGenes, NeoplasmTranscription, GeneticAnimalsB-LymphocytesBromodomain Containing ProteinsCell CycleChromosomal Proteins, Non-HistoneHumansLymphoma, B-CellMiceMice, TransgenicProtein Serine-Threonine KinasesTranscription FactorsTranscription Factor TFIIDBrd2 protein, mouseBromodomain Containing ProteinsChromosomal Proteins, Non-HistoneProtein Serine-Threonine KinasesTranscription FactorsTranscription Factor TFIID

Identifiers

PMID17166848
PMCPMC2819333
OpenAlexW1986575341

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.